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“DIESSE” CHORUS TOXOPLASMA IgG AVIDITY - Taiwan Registration d447749b85367da245415e4216335fb5

Access comprehensive regulatory information for “DIESSE” CHORUS TOXOPLASMA IgG AVIDITY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d447749b85367da245415e4216335fb5 and manufactured by DIESSE DIAGNOSTICA SENESE S.P.A.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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d447749b85367da245415e4216335fb5
Registration Details
Taiwan FDA Registration: d447749b85367da245415e4216335fb5
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Device Details

“DIESSE” CHORUS TOXOPLASMA IgG AVIDITY
TW: “迪雅仕” 可錄思 弓漿蟲IgG抗體親和力試劑組
Risk Class 2
MD

Registration Details

d447749b85367da245415e4216335fb5

Ministry of Health Medical Device Import No. 026756

DHA05602675601

Company Information

Product Details

This product is used with the Chorus system to qualitatively detect anti-toxoplasmosis IgG antibodies in human serum.

C Immunology and microbiology devices

C3780 Toxoplasma rodent serum reagent

Imported from abroad

Dates and Status

Dec 04, 2014

Dec 04, 2024